PT773955E - NEW TROMBIN INHIBITORS AND THEIR MANUFACTURE AND USES - Google Patents
NEW TROMBIN INHIBITORS AND THEIR MANUFACTURE AND USESInfo
- Publication number
- PT773955E PT773955E PT95923231T PT95923231T PT773955E PT 773955 E PT773955 E PT 773955E PT 95923231 T PT95923231 T PT 95923231T PT 95923231 T PT95923231 T PT 95923231T PT 773955 E PT773955 E PT 773955E
- Authority
- PT
- Portugal
- Prior art keywords
- manufacture
- new
- trombin
- inhibitors
- compounds
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0812—Tripeptides with the first amino acid being neutral and aromatic or cycloaliphatic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/62—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid
- A61K47/64—Drug-peptide, drug-protein or drug-polyamino acid conjugates, i.e. the modifying agent being a peptide, protein or polyamino acid which is covalently bonded or complexed to a therapeutically active agent
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/04—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/46—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with hetero atoms directly attached to the ring nitrogen atom
- C07D207/48—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/60—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06017—Dipeptides with the first amino acid being neutral and aliphatic
- C07K5/06026—Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atom, i.e. Gly or Ala
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06017—Dipeptides with the first amino acid being neutral and aliphatic
- C07K5/0606—Dipeptides with the first amino acid being neutral and aliphatic the side chain containing heteroatoms not provided for by C07K5/06086 - C07K5/06139, e.g. Ser, Met, Cys, Thr
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06078—Dipeptides with the first amino acid being neutral and aromatic or cycloaliphatic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06104—Dipeptides with the first amino acid being acidic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06104—Dipeptides with the first amino acid being acidic
- C07K5/06113—Asp- or Asn-amino acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Abstract
Compounds of the formula and the salts thereof with physiologically tolerated acids and the stereoisomers thereof, in which the substituents have the meanings stated in the description, are described. Also disclosed are intermediates for their preparation. The compounds are suitable for controlling diseases.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4421052A DE4421052A1 (en) | 1994-06-17 | 1994-06-17 | New thrombin inhibitors, their production and use |
Publications (1)
Publication Number | Publication Date |
---|---|
PT773955E true PT773955E (en) | 2003-09-30 |
Family
ID=6520741
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PT95923231T PT773955E (en) | 1994-06-17 | 1995-06-06 | NEW TROMBIN INHIBITORS AND THEIR MANUFACTURE AND USES |
Country Status (26)
Country | Link |
---|---|
US (3) | US6455671B1 (en) |
EP (1) | EP0773955B1 (en) |
JP (1) | JPH10501541A (en) |
CN (1) | CN1189476C (en) |
AT (1) | ATE237631T1 (en) |
AU (1) | AU699501B2 (en) |
BR (1) | BR9508057A (en) |
CA (1) | CA2193133A1 (en) |
CZ (1) | CZ293426B6 (en) |
DE (2) | DE4421052A1 (en) |
DK (1) | DK0773955T3 (en) |
ES (1) | ES2197200T3 (en) |
FI (1) | FI965039A (en) |
HR (1) | HRP950338B1 (en) |
HU (1) | HUT78040A (en) |
IL (1) | IL114127A (en) |
MX (1) | MX9606521A (en) |
NO (1) | NO965412L (en) |
NZ (1) | NZ288591A (en) |
PL (1) | PL181405B1 (en) |
PT (1) | PT773955E (en) |
RU (1) | RU2172741C2 (en) |
SI (1) | SI9520075B (en) |
TW (1) | TW458986B (en) |
WO (1) | WO1995035309A1 (en) |
ZA (1) | ZA954972B (en) |
Families Citing this family (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5707966A (en) * | 1994-03-04 | 1998-01-13 | Eli Lilly And Company | Antithrombotic agents |
US5726159A (en) * | 1994-03-04 | 1998-03-10 | Eli Lilly And Company | Antithrombotic agents |
US5705487A (en) * | 1994-03-04 | 1998-01-06 | Eli Lilly And Company | Antithrombotic agents |
PL321759A1 (en) * | 1995-02-17 | 1997-12-22 | Basf Ag | Novel thrombosin inhibitors |
US5710130A (en) * | 1995-02-27 | 1998-01-20 | Eli Lilly And Company | Antithrombotic agents |
US5914319A (en) * | 1995-02-27 | 1999-06-22 | Eli Lilly And Company | Antithrombotic agents |
CA2176414A1 (en) * | 1995-05-18 | 1996-11-19 | S. David Kimball | Acyl guanidine and amidine prodrugs |
SA96170106A (en) | 1995-07-06 | 2005-12-03 | أسترا أكتيبولاج | New amino acid derivatives |
TWI238827B (en) * | 1995-12-21 | 2005-09-01 | Astrazeneca Ab | Prodrugs of thrombin inhibitors |
GB9526273D0 (en) * | 1995-12-21 | 1996-02-21 | Astra Ab | New prodrugs |
CA2239711A1 (en) * | 1995-12-22 | 1997-07-03 | Novo Nordisk A/S | Compounds with growth hormone releasing properties |
US5942544A (en) * | 1996-02-22 | 1999-08-24 | Dupont Pharmaceuticals Company | α-branched anilines, toluenes, and analogs thereof as factor Xa inhibitors |
US5811402A (en) * | 1996-03-22 | 1998-09-22 | Eli Lilly And Company | Antithrombotic diamides |
KR100483869B1 (en) * | 1996-06-07 | 2005-09-09 | 아스트라제네카 악티에볼라그 | New Amino Acid Derivatives and Their Use as Thrombin Inhibitors |
SE9602263D0 (en) * | 1996-06-07 | 1996-06-07 | Astra Ab | New amino acid derivatives |
US6200967B1 (en) | 1996-06-25 | 2001-03-13 | Eli Lilly And Company | Anticoagulant agents |
JP2000514788A (en) * | 1996-06-25 | 2000-11-07 | イーライ・リリー・アンド・カンパニー | Anticoagulant |
SE9602646D0 (en) | 1996-07-04 | 1996-07-04 | Astra Ab | Pharmaceutically useful compounds |
DE19632772A1 (en) | 1996-08-14 | 1998-02-19 | Basf Ag | New benzamidines |
DE19632773A1 (en) * | 1996-08-14 | 1998-02-19 | Basf Ag | New thrombin inhibitors |
AR013084A1 (en) | 1997-06-19 | 2000-12-13 | Astrazeneca Ab | USEFUL AMIDINE DERIVATIVES AS THROMBIN INHIBITORS, PHARMACEUTICAL COMPOSITION, USE OF SUCH COMPOUNDS FOR THE PREPARATION OF MEDICINES AND THE PROCESS FOR THE PREPARATION OF THE MENTIONED COMPOUNDS |
SE9704543D0 (en) | 1997-12-05 | 1997-12-05 | Astra Ab | New compounds |
AU751111B2 (en) * | 1998-01-26 | 2002-08-08 | Basf Aktiengesellschaft | Thrombin inhibitors |
US6291514B1 (en) * | 1998-02-09 | 2001-09-18 | 3-Dimensional Pharmaceuticals, Inc. | Heteroaryl amidines, methylamidines and guanidines, preparation thereof, and use thereof as protease inhibitors |
EP1073449A4 (en) | 1998-04-24 | 2003-01-02 | Dimensional Pharm Inc | Amino acid amidinohydrazones, alkoxyguanidines and aminoguanidines as protease inhibitors |
SE9804313D0 (en) | 1998-12-14 | 1998-12-14 | Astra Ab | New compounds |
US6599894B1 (en) | 1999-01-13 | 2003-07-29 | AstŕaZeneca AB | Amidinobenzylamine derivatives and their use as thrombin inhibitors |
MXPA01010114A (en) | 1999-04-09 | 2002-07-30 | Basf Ag | Low-molecular inhibitors of complement proteases. |
PL352834A1 (en) * | 1999-04-09 | 2003-09-08 | Abbott Gmbh & Co.Kg | Prodrugs of thrombin inhibitors |
AR023510A1 (en) | 1999-04-21 | 2002-09-04 | Astrazeneca Ab | A TEAM OF PARTS, PHARMACEUTICAL FORMULATION AND USE OF A THROMBIN INHIBITOR. |
SE0001803D0 (en) | 2000-05-16 | 2000-05-16 | Astrazeneca Ab | New compounds i |
US6433186B1 (en) | 2000-08-16 | 2002-08-13 | Astrazeneca Ab | Amidino derivatives and their use as thormbin inhibitors |
DE10049937A1 (en) * | 2000-10-06 | 2002-04-11 | Knoll Ag | New sugar-modified amidine and guanidine compounds, useful as competitive inhibitors of serine protease, e.g. for treating thrombosis |
US7129233B2 (en) | 2000-12-01 | 2006-10-31 | Astrazeneca Ab | Mandelic acid derivatives and their use as thrombin inhibitors |
AR035216A1 (en) | 2000-12-01 | 2004-05-05 | Astrazeneca Ab | MANDELIC ACID DERIVATIVES, PHARMACEUTICALLY ACCEPTABLE DERIVATIVES, USE OF THESE DERIVATIVES FOR THE MANUFACTURE OF MEDICINES, TREATMENT METHODS, PROCESSES FOR THE PREPARATION OF THESE DERIVATIVES, AND INTERMEDIARY COMPOUNDS |
DE10064797A1 (en) * | 2000-12-22 | 2002-06-27 | Knoll Ag | Combination pack useful for the treatment of e.g. deep vein thrombosis and post-operative thrombosis, containing oral and parenteral formulations of thrombin inhibitor prodrugs |
DE10117730A1 (en) * | 2001-04-09 | 2002-10-10 | Basf Ag | One-pot reaction of amines, useful for preparing e.g. cyclic secondary amines or alcohols, useful as pharmaceutical intermediates, by oxidation with lysine oxidase then reduction |
AR034517A1 (en) | 2001-06-21 | 2004-02-25 | Astrazeneca Ab | PHARMACEUTICAL FORMULATION |
SE0201661D0 (en) | 2002-05-31 | 2002-05-31 | Astrazeneca Ab | New salts |
SE0201659D0 (en) | 2002-05-31 | 2002-05-31 | Astrazeneca Ab | Modified release pharmaceutical formulation |
US7781424B2 (en) * | 2003-05-27 | 2010-08-24 | Astrazeneca Ab | Modified release pharmaceutical formulation |
US7795205B2 (en) * | 2004-04-12 | 2010-09-14 | Canyon Pharmaceuticals, Inc. | Methods for effecting regression of tumor mass and size in a metastasized pancreatic tumor |
US8257648B2 (en) | 2004-12-21 | 2012-09-04 | Scott Elrod | System and method for reducing odors in a blind |
DE102005025728A1 (en) * | 2005-06-04 | 2006-12-07 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Polymorphs of 3 - [(2 - {[4- (hexyloxycarbonylamino-imino-methyl) -phenyl-amino] -methyl} -1-methyl-1H-benzimidazole-5-carbonyl) -pyridin-2-yl-amino] -propionic acid ethyl ester |
US7524354B2 (en) * | 2005-07-07 | 2009-04-28 | Research Foundation Of State University Of New York | Controlled synthesis of highly monodispersed gold nanoparticles |
TW200827336A (en) | 2006-12-06 | 2008-07-01 | Astrazeneca Ab | New crystalline forms |
US20090061000A1 (en) * | 2007-08-31 | 2009-03-05 | Astrazeneca Ab | Pharmaceutical formulation use 030 |
WO2011120040A2 (en) * | 2010-03-26 | 2011-09-29 | Matrix Pharma Inc. | Thrombin inhibiting compositions |
JP2012049597A (en) * | 2010-08-24 | 2012-03-08 | Nikon Corp | Imaging apparatus |
Family Cites Families (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
HU178398B (en) | 1979-06-12 | 1982-04-28 | Gyogyszerkutato Intezet | Process for producing new agmatine derivatives of activity against haemagglutination |
GB8305985D0 (en) | 1983-03-04 | 1983-04-07 | Szelke M | Enzyme inhibition |
HU192646B (en) | 1984-12-21 | 1987-06-29 | Gyogyszerkutato Intezet | Process for preparing new n-alkyl-peptide aldehydes |
IL77748A (en) | 1985-02-04 | 1991-11-21 | Merrell Dow Pharma | Amino acid and peptide derivatives as peptidase inhibitors |
US5187157A (en) | 1987-06-05 | 1993-02-16 | Du Pont Merck Pharmaceutical Company | Peptide boronic acid inhibitors of trypsin-like proteases |
EP0362002B1 (en) | 1988-09-01 | 1995-07-26 | Merrell Dow Pharmaceuticals Inc. | HIV protease inhibitors |
ZA897515B (en) | 1988-10-07 | 1990-06-27 | Merrell Dow Pharma | Novel peptidase inhibitors |
CA2021660A1 (en) | 1989-07-26 | 1991-01-27 | Philippe Bey | Peptidase inhibitors |
GB9017694D0 (en) | 1990-08-13 | 1990-09-26 | Sandoz Ltd | Improvements in or relating to organic chemistry |
IL99527A (en) | 1990-09-28 | 1997-08-14 | Lilly Co Eli | Tripeptide antithrombotic agents |
SE9003534D0 (en) | 1990-11-06 | 1990-11-06 | Kabigen Ab | A METHOD FOR ISOLATING AND PURIFYING PEPTIDES AND PROTEINS |
JPH05503300A (en) * | 1990-11-15 | 1993-06-03 | ペンタファルム アクチェンゲゼルシャフト | Meta-substituted phenylalanine derivatives |
EP0503203A1 (en) | 1991-03-15 | 1992-09-16 | Merrell Dow Pharmaceuticals Inc. | Novel thrombin inhibitors |
DE4115468A1 (en) * | 1991-05-11 | 1992-11-12 | Behringwerke Ag | AMIDINOPHENYLALANINE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF, THE USE THESE AND THE MEANS THEREOF CONTAINING ANTICOAGULANTS |
CA2075154A1 (en) | 1991-08-06 | 1993-02-07 | Neelakantan Balasubramanian | Peptide aldehydes as antithrombotic agents |
SE9102462D0 (en) | 1991-08-28 | 1991-08-28 | Astra Ab | NEW ISOSTERIC PEPTIDES |
NZ245039A (en) | 1991-11-12 | 1994-12-22 | Lilly Co Eli | N-phenylalanyl and n-phenylglycyl derivatives of the dipeptide of l-azetidine-2-carboxylic acid and l-arginine aldehyde; anti-blood clotting compositions |
SE9103612D0 (en) | 1991-12-04 | 1991-12-04 | Astra Ab | NEW PEPTIDE DERIVATIVES |
ATE171709T1 (en) | 1992-02-14 | 1998-10-15 | Corvas Int Inc | INHIBITORS OF THROMBOSIS |
JPH08501057A (en) | 1992-03-04 | 1996-02-06 | ヂョヂセルクタトー インテーゼット カーエフテー | Novel anticoagulant factor peptide derivative, pharmaceutical composition containing the same, and method for producing the same |
FR2695562B1 (en) | 1992-09-11 | 1994-10-14 | Synthelabo | Use of a direct thrombin inhibitor for the manufacture of a medicament with thrombolytic activity. |
US5371072A (en) | 1992-10-16 | 1994-12-06 | Corvas International, Inc. | Asp-Pro-Arg α-keto-amide enzyme inhibitors |
AU675981B2 (en) | 1992-12-02 | 1997-02-27 | Bristol-Myers Squibb Company | Guanidinyl-substituted heterocyclic thrombin inhibitors |
SE9301916D0 (en) * | 1993-06-03 | 1993-06-03 | Ab Astra | NEW PEPTIDES DERIVATIVES |
US5783563A (en) | 1993-06-03 | 1998-07-21 | Astra Aktiebolag | Method for treatment or prophylaxis of venous thrombosis |
EP0648780A1 (en) | 1993-08-26 | 1995-04-19 | Bristol-Myers Squibb Company | Heterocyclic thrombin inhibitors |
CA2140598C (en) | 1994-01-27 | 2010-03-09 | Masahiro Ohshima | Prolineamide derivatives |
US5726159A (en) | 1994-03-04 | 1998-03-10 | Eli Lilly And Company | Antithrombotic agents |
ZA951617B (en) | 1994-03-04 | 1997-02-27 | Lilly Co Eli | Antithrombotic agents. |
US5705487A (en) | 1994-03-04 | 1998-01-06 | Eli Lilly And Company | Antithrombotic agents |
US5710130A (en) | 1995-02-27 | 1998-01-20 | Eli Lilly And Company | Antithrombotic agents |
GB2302231B (en) * | 1995-03-14 | 1999-01-13 | Matsushita Electric Ind Co Ltd | Speaker system |
-
1994
- 1994-06-17 DE DE4421052A patent/DE4421052A1/en not_active Withdrawn
-
1995
- 1995-06-06 RU RU97100941/04A patent/RU2172741C2/en not_active IP Right Cessation
- 1995-06-06 EP EP95923231A patent/EP0773955B1/en not_active Revoked
- 1995-06-06 WO PCT/EP1995/002135 patent/WO1995035309A1/en not_active Application Discontinuation
- 1995-06-06 NZ NZ288591A patent/NZ288591A/en not_active IP Right Cessation
- 1995-06-06 HU HU9603474A patent/HUT78040A/en unknown
- 1995-06-06 BR BR9508057A patent/BR9508057A/en not_active Application Discontinuation
- 1995-06-06 CZ CZ19963713A patent/CZ293426B6/en not_active IP Right Cessation
- 1995-06-06 SI SI9520075A patent/SI9520075B/en not_active IP Right Cessation
- 1995-06-06 DE DE59510645T patent/DE59510645D1/en not_active Revoked
- 1995-06-06 CN CNB951942123A patent/CN1189476C/en not_active Expired - Fee Related
- 1995-06-06 CA CA002193133A patent/CA2193133A1/en not_active Abandoned
- 1995-06-06 PT PT95923231T patent/PT773955E/en unknown
- 1995-06-06 JP JP8501568A patent/JPH10501541A/en active Pending
- 1995-06-06 US US08/682,604 patent/US6455671B1/en not_active Expired - Lifetime
- 1995-06-06 AU AU27875/95A patent/AU699501B2/en not_active Ceased
- 1995-06-06 AT AT95923231T patent/ATE237631T1/en not_active IP Right Cessation
- 1995-06-06 DK DK95923231T patent/DK0773955T3/en active
- 1995-06-06 ES ES95923231T patent/ES2197200T3/en not_active Expired - Lifetime
- 1995-06-06 MX MX9606521A patent/MX9606521A/en not_active IP Right Cessation
- 1995-06-06 PL PL95317989A patent/PL181405B1/en not_active IP Right Cessation
- 1995-06-13 IL IL11412795A patent/IL114127A/en not_active IP Right Cessation
- 1995-06-14 HR HR950338A patent/HRP950338B1/en not_active IP Right Cessation
- 1995-06-15 ZA ZA954972A patent/ZA954972B/en unknown
- 1995-06-16 TW TW084106192A patent/TW458986B/en active
-
1996
- 1996-12-16 FI FI965039A patent/FI965039A/en not_active IP Right Cessation
- 1996-12-16 NO NO965412A patent/NO965412L/en not_active Application Discontinuation
-
2002
- 2002-04-29 US US10/133,384 patent/US20030004308A1/en not_active Abandoned
-
2004
- 2004-10-25 US US10/973,643 patent/US20060111553A1/en not_active Abandoned
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